AY-NH2

Pricing Availability   Qty
说明: Selective PAR4 agonist
别名: AYPGKF-NH2
纯度: ≥95% (HPLC)
说明书
引用文献 (4)
评论

生物活性 for AY-NH2

AY-NH2 is a selective PAR4 receptor agonist peptide. Stimulates platelet aggregation in vitro (EC50 = 15 μM). Exhibits an increase in paw thickness in the paw edema inflammation model in vivo.

技术数据 for AY-NH2

分子量 680.8
公式 C34H48N8O7
序列 AYPGKF

(Modifications: Phe-6 = C-terminal amide)

储存 Store at -20°C
纯度 ≥95% (HPLC)
CAS Number 352017-71-1
PubChem ID 9987061
InChI Key BBAOHIALRKLBRD-OZDPOCAXSA-N
Smiles [H]N[C@@H](C)C(=O)N[C@@H](CC1=CC=C(O)C=C1)C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC1=CC=CC=C1)C(N)=O

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for AY-NH2

溶解性 Soluble to 2 mg/ml in water

产品说明书 for AY-NH2

分析证书/产品说明书
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参考文献 for AY-NH2

参考文献是支持产品生物活性的出版物。

Faruqi et al (2000) Structure-function analysis of protease-activated receptor 4 tethered ligand peptides. J.Biol.Chem. 275 19728 PMID: 10779527

Hollenberg and Saifeddine (2001) Proteinase-activated receptor 4 (PAR4): activation and inhibition of rat platelet aggregation by PAR4-derived peptides. Can.J.Physiol.Pharmacol. 79 439 PMID: 11405248

Hollenburg et al (2004) Proteinase-activated receptor-4: evaluation of tethered ligand-derived peptides as probes for receptor function and as inflammatory agonists in vivo. Br.J.Pharmacol. 143 443 PMID: 15451771


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关键词: AY-NH2, AY-NH2 supplier, selective, PAR4, agonists, receptors, protease-activated, proteinase-activated, peptide, AYPGKF-NH2, Protease-Activated, Receptors, 1487, Tocris Bioscience

4 篇 AY-NH2 的引用文献

引用文献是使用了 Tocris 产品的出版物。 AY-NH2 的部分引用包括:

de la Fuente et al (2020) Expression and Purification of Protease-Activated Receptor 4 (PAR4) and Analysis with Histidine Hydrogen-Deuterium Exchange. Biochemistry 59 671 PMID: 31957446

Peng et al (2019) Protease Activated Receptor 4 as a Novel Modulator of Regulatory T Cell Function. Front Immunol 10 1311 PMID: 31275306

Wang (2017) Complement-activation fragment C4a mediates effector functions by binding as untethered agonist to protease-activated receptors 1 and 4. Proc Natl Acad Sci U S A 114 10948 PMID: 28973891

Shi et al (2015) Alterations in serotonin, transient receptor potential channels and protease-activated receptors in rats with irritable bowel syndrome attenuated by Shugan decoction. Oncogene 21 4852 PMID: 25944998


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